首页> 外文期刊>Investigative ophthalmology & visual science >Using pharmacy claims data to study adherence to glaucoma medications: methodology and findings of the Glaucoma Adherence and Persistency Study (GAPS).
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Using pharmacy claims data to study adherence to glaucoma medications: methodology and findings of the Glaucoma Adherence and Persistency Study (GAPS).

机译:使用药房索赔数据研究对青光眼药物的依从性:青光眼依从性和持久性研究(GAPS)的方法和结果。

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PURPOSE: To develop methods for investigating adherence to glaucoma medications by using a modified claims data-based measure of adherence, validation by chart review, and patient and physician interviews. METHODS: Data from administrative claims of 13,956 subjects receiving an initial glaucoma medication, and data from overlapping samples of 300 patients' charts, 300 interviews of patients, and 103 interviews of physicians were analyzed and compared. RESULTS: The mean medication possession ratio (MPR) was 0.64 (median 0.57) for the 13,956 subjects. Although 59% potentially had an ocular hypotensive agent at 12 months, only 10% had such medication available continuously. Chart review revealed that 31% of subjects "new to therapy" in claims data had actually been previously treated; and that 90% of the 17% who had medication added to initial monotherapy were misclassified by claims-based algorithms as medication switches or no change. Twenty percent of surveyed patients received samples on a regular basis and had lower MPR than those who did not (P < 0.05). CONCLUSIONS: Large pharmacy databases offer insight into medication usage but are vulnerable to errors from sampling (since patients who receive samples will be considered to have poor adherence), misidentification of newly treated patients, and misclassification of added versus switched medications. That a large proportion of patients stop and restart medications makes MPR a robust measure of adherence over time that reflects the resumption of medication after a gap in adherence. The data confirm that adherence to treatment with glaucoma medications is poor, similar to adherence in patients with other chronic diseases.
机译:目的:通过使用改良的基于索赔数据的依从性度量,通过图表检查进行验证以及患者和医师访谈来开发调查青光眼药物依从性的方法。方法:分析和比较了13956名接受青光眼治疗的受试者的行政索赔数据,以及300例患者图表,300例患者访谈和103例医生访谈的重叠样本中的数据。结果:13956名受试者的平均药物拥有率(MPR)为0.64(中位数0.57)。尽管59%的患者在12个月时可能有降眼压药,但只有10%的患者连续可使用这种药物。图表审查显示,索赔数据中有31%的“刚接受治疗的新人”实际上曾接受过治疗;在最初的单一疗法中增加药物治疗的17%患者中,有90%被基于索赔的算法错误归类为药物转换或不变。被调查的患者中有20%定期接受样本,其MPR低于未接受抽样的患者(P <0.05)。结论:大型药房数据库提供了药物使用情况的信息,但容易受到抽样错误的影响(因为接受样品的患者将被认为依从性差),新治疗患者的错误识别以及添加和转换药物的错误分类。大量患者停止和重新开始用药,使MPR成为随时间推移依从性的有力衡量标准,反映了依从性差后药物的恢复。数据证实,青光眼药物治疗依从性差,类似于其他慢性疾病患者的依从性。

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